- Daiichi Sankyo, Inc. (Bernards, NJ)
- …for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... research areas centered around rare diseases and immune disorders. Summary The Manager , Clinical Data Standards is responsible for the development and sustainability… more
- Novo Nordisk Inc. (Plainsboro, NJ)
- …pharmaceutical industry Minimum 2 years of experience as a Clinical Trial/Project Manager Experience with global clinical trial operations, in multiple phases ... About the Department Our East Coast Global Development Hub brings together the best minds...Position We are looking to hire a Clinical Project Manager (CPM). This is a unique opportunity to work… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …medicines to help people. Under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... research areas centered around rare diseases and immune disorders. Summary The Manager External Data Management, is accountable for an end-to-end delivery of… more
- Aequor (Thousand Oaks, CA)
- …across all functions.Responsibilities:Lead medium/small projects independently and work directly with Program Manager on large multi-year programs. Managing the ... functional goals, execution adjustments/iterations, and cross-functional teamwork. Works with the Program Manager to ensure effective and efficient communication… more
- Daiichi Sankyo, Inc. (Bernards, NJ)
- …for cardiovascular diseases, under the Group's 2025 Vision to become a " Global Pharma Innovator with Competitive Advantage in Oncology," Daiichi Sankyo is primarily ... ensure they meet the needs of the business and regulatory requirements.- Collaborate with business units to identify opportunities...Vision Road Map Development- Partner with both regional and global business along with DX/IT teams to develop, own… more
- Merck & Co. (Rahway, NJ)
- …and execution of Phase 1-4 clinical studies. Under the direction of the Program Lead, you will collaborate with global , cross-functional team members including ... clinical trial team.Collaborates with the Medical Writer on clinical/scientific and regulatory documents. Partners with Study Manager on study… more
- Merck & Co. (Millsboro, DE)
- …animal facilities as well as for the veterinary care and animal husbandry program at our company's Millsboro Animal Health facilities. This role is highly ... documentation, and other information as needed for annual reports to Federal regulatory agencies. Leadership for internal and external regulatory inspections… more
- Merck & Co. (Rahway, NJ)
- …strategy and execution of Phase 1-4 clinical studies. Under the direction of the Program Lead, you will collaborate with global , cross -functional team members ... trial team.Collaborates with the Medical Writer on clinical/scientific and regulatory documents.Partners with Study Manager on study deliverables.Participates… more
- Aequor (Thousand Oaks, CA)
- …partners with the FDP manufacturing network, quality, engineering, external supply and global logistics in developing the necessary set of actions to meet the ... business objectives; Commercialization and Transformation, strategizes commercial and pipeline program expertise, leads transformational operations, and drives business for… more
- Eclaro (Hamilton Square, NJ)
- …WWPS needs. The PV Analytics and Reporting Specialist reports to the Senior Manager , PV Analytics Center of Excellence, within Global Biostatistics & Data ... activities aligned with the overall vision, strategy, and objectives of the Global Biostatistics & Data Sciences Function. The PV Analytics and Reporting Specialist,… more
- Amazon (Bellevue, WA)
- … global program . We are looking for a talented program manager who has experience with global consumer product regulations to support our rapidly ... is looking for a smart, energetic, hard-working, and creative Program Manager to join our team. The...program focusing on US and Canada Trade and Regulatory programs. By supporting compliance approaches while creating innovative… more
- HSBC (New York, NY)
- …our people, our investors, our communities and the planet we all share. A Global Regulatory Policy Manager - Liquidity provides technical regulatory ... challenge and governance to mitigate regulatory risk. Global Regulatory Policy Manager -...through an industry-leading volunteerism policy, a generous matching gift program , and a comprehensive program of immersive… more
- Olympus Corporation of the Americas (Westborough, MA)
- …agencies regarding compliance issues. Leads and manages the development of all global regulatory communication processes to include responses external audits, ... Duties** + Authors, leads and manages the development of global regulatory communication processes to include responses...room and back room would be a plus. + Program management experience managing multiple programs and projects to… more
- AbbVie (North Chicago, IL)
- …you will be added to our talent pipeline and considered for future opportunities. Global Regulatory Affairs Strategy roles (US and Canada) are: 1. Responsible ... for products within a Therapeutic Area & support the Global Regulatory Lead (GRL) & Therapeutic Area...regulations, company policies, procedures, & guidance in alignment with regulatory product strategy & Quality Dossier Program … more
- Berry Global (Evansville, IN)
- …LinkedIn or Twitter. **Position Summary:** The Global Mobility & Immigration Senior Program Manager will oversee and manage the Company's global mobility ... other federal, state or local protected class. (https://careers-berryglobal.icims.com/jobs/26297/ global -mobility-%26-immigration-senior- program - manager /job?mode=apply&apply=yes&in\_iframe=1&hashed=-1834445335) **Location** _US-IN-EVANSVILLE_… more
- Teva Pharmaceuticals (Parsippany, NJ)
- Director, Therapy Area Head, Global Regulatory Medical Writing (USA, Remote) Date: Nov 17, 2024 Location: Parsippany, United States, New Jersey, 07005 Company: ... enable people to live better, healthier lives. **The opportunity** As a **Director, in Global Regulatory Medical Writing (GRMW)** , you will primarily work in a… more
- Bank of America (Charlotte, NC)
- …Plan, coordinate and manage the day-to-day execution of the Global Regulatory Reporting In-Line Quality Assurance program and develop a sustainable operating ... Quality Assurance Lead for Global Regulatory Reporting - US Charlotte,...performance, success criteria and results of the in-line QA program + Identify opportunities to deliver continuous improvement to… more
- Olympus Corporation of the Americas (Westborough, MA)
- … Body contact. **Job Duties** + Authors and manages the development of global additional information regulatory communication processes to include responses to ... implementation of Global Customer Quality initiatives and programs throughout the Global organization, as required. + Site MDR/ Regulatory Body Contact. +… more
- Bank of America (Charlotte, NC)
- …coordination and management of the day-to-day execution of the Global Regulatory Reporting In-Line Quality Assurance program and develop a sustainable ... Quality Assurance Specialist for Global Regulatory Reporting - US Charlotte,...for this role is assist the Quality Assurance (QA) manager in the build out of the function for… more
- Takeda Pharmaceuticals (Lexington, MA)
- …and approves - as needed - technical protocols, reports, etc. to ensure alignment with global regulatory requirements and standards. + When in a GRA CMC Product ... according to agreed business priorities. + As a line manager role, provides project and administrative oversight to support...regulatory guidance to product teams in line with global regulatory strategies. Accountable for development and… more
